Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

3701–3725 of 5038

SevereFDA (Devices)·Z-1509-2017·2017-03-29
Ohmeda Medical Recalls Giraffe OmniBed Infant Incubators Due to Fire Risk
Ohmeda Medical is recalling Giraffe OmniBed infant incubators and warmers because certain power cords may overheat, posing a risk of fire or thermal injury.
Product
Giraffe OmniBed Ohmeda Medical Omnibed- The OmniBed is a combination of an infant incubator ( incubator ) and an infant radiant warmer ( warmer ). Incubators and warmers provide heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiolo
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1503-2017·2017-03-29
Ohmeda Medical Spot PT Lite Phototherapy System Recalled for Power Cord Fire Risk
Ohmeda Medical is recalling Spot PT Lite Phototherapy Systems because certain power cords could overheat, posing a risk of fire or thermal injury.
Product
Giraffe Spot PT Ohmeda Medical Spot PT Lite Phototherapy System- The Spot PT Lite Phototherapy System provides light therapy for the treatment of hyperbilirubinemia, commonly known as neonatal jaundice, during the newborn period in the hospital
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1507-2017·2017-03-29
Ohmeda Infant Warmers Recalled Due to Power Cord Overheating Risk
Ohmeda Medical is recalling Giraffe and Panda infant radiant warmers because certain power cords may overheat, posing a fire or thermal injury risk.
Product
Giraffe Bedded Warmer, Panda Warmer Modification to Giraffe and Panda Warmers (Giraffe and Panda Uninterruptible Power Supply) - Infant radiant warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Infan
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1505-2017·2017-03-29
Ohmeda Medical Recalls Giraffe Incubators Due to Power Cord Overheating
Ohmeda Medical is recalling Giraffe Incubators because certain power cords may overheat, posing a risk of fire or thermal injury.
Product
Giraffe Incubator Ohmeda Medical Giraffe Incubator-The Giraffe Incubator is an infant incubator. Incubators provide heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. They achieve this by providing an enclosed temperature con
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1506-2017·2017-03-29
Ohmeda Infant Radiant Warmers Recalled for Power Cord Overheating Risk
Ohmeda Medical is recalling Giraffe and Panda infant radiant warmers because certain power cords may overheat, posing a fire or thermal injury risk.
Product
Giraffe Bedded Warmer, Panda Warmer Giraffe and Panda Warmer- Infant radiant warmers provide infrared heat in a controlled manner to neonates who are unable to thermoregulate based on their own physiology. Infant radiant warmers may be used to facilitate the neonate's transition
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1504-2017·2017-03-29
Ohmeda Medical Recalls Giraffe OmniBed Infant Incubators Due to Fire Risk
Ohmeda Medical is recalling Giraffe OmniBed infant incubators and warmers because certain power cords may overheat, posing a risk of fire or thermal injury.
Product
Giraffe OmniBed Ohmeda Medical Giraffe OmniBed- The OmniBed is a combination of an infant incubator and an infant warmer. The device can be operated as an incubator or as a warmer and can transition from one mode to the other on user s demand. It cannot be operated in both modes
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1508-2017·2017-03-29
Ohmeda Infant Radiant Warmers Recalled for Power Cord Overheating Risk
Ohmeda Medical is recalling Giraffe and Panda infant radiant warmers because certain power cords could overheat, posing a risk of fire or thermal injury.
Product
Giraffe Bedded Warmer, Panda Warmer Modifiction to Giraffe and Panda Warmer- Infant radiant warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Infant radiant warmers may be used to facilitate the neon
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1460-2017·2017-03-22
Arkon Anesthesia Delivery System Recalled for Unannounced Power Supply Failure
Del Mar Reynolds Medical is recalling Arkon Anesthesia Delivery Systems because the power supply can fail without triggering normal battery alarms.
Product
Arkon Anesthesia Delivery System, Model 99999. Product Usage: Continuous Ventilator The Arkon Anesthesia Delivery System is designed to provide emergency oxygen, vaporized agent delivery and manual ventilation in the event of a power failure scenario. Clinicians are able to
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1257-2017·2017-03-15
Physio-Control Recalls LIFEPAK 1000 Defibrillators for Unexpected Power-Offs
Physio-Control is recalling 133,330 LIFEPAK 1000 defibrillators worldwide because they may unexpectedly power off during use.
Product
The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1433-2017·2017-03-15
Siemens Medical Recalls 35 MEVATRON M 6700 Linear Accelerators
Siemens Medical Solutions USA is recalling 35 MEVATRON M 6700 linear accelerators due to a defective weld seam that could cause the overhead suspension to fall and injure a patient or other person.
Product
MEVATRON M 6700 (MX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1429-2017·2017-03-15
Apollo DRF X-ray Systems Recalled Due to Footrest Detachment Hazard
Villa Sistemi Medicali is recalling 65 Apollo DRF x-ray systems because the footrest can detach, causing patients to fall from the table.
Product
Apollo DRF; Model: 9784220831 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1432-2017·2017-03-15
Siemens PRIMUS HI and Mevatron M2 Linear Accelerators Recalled for Weld Defect
Siemens is recalling 35 PRIMUS HI and Mevatron M2 linear accelerators due to a defective weld seam that could cause overhead suspensions to fall and injure people.
Product
PRIMUS HI and Mevatron M2/Primus Mid-Energy, Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1428-2017·2017-03-15
Villa Sistemi Medicali Recalls Apollo X-Ray Systems Due to Footrest Detachment
Villa Sistemi Medicali is recalling 65 Apollo multi-function x-ray systems because the footrest detached from the table, causing a patient to fall.
Product
Apollo; Models: 9784000131 9784000231 9784020131 9784020231 9784100231 9784120131 9784120231 9784130131 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1437-2017·2017-03-15
Siemens MEVATRON KD-2 Linear Accelerators Recalled for Defective Weld Seams
Siemens is recalling 35 MEVATRON KD-2 linear accelerators due to defective weld seams that could break and cause the overhead suspension to fall, posing a risk of severe injury.
Product
MEVATRON KD-2, accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1408-2017·2017-03-15
FDA Recalls Premier Guard Sterile Drapes Due to Sterility Compromise
The FDA is recalling Premier Guard Sterile Drapes because the sterile barrier was breached, compromising sterility. The recall covers 1,111,600 units distributed nationwide.
Product
Premier Guard Sterile Drape For Use with Blair-Port Wand (02-0029) and Blair-Port Wand X (01-0046) Item Number: 01-0020 Used in conjunction RF Surgical Gauze detection systems to protect scanning device from contamination during various surgical procedures
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1436-2017·2017-03-15
Siemens Medical Linear Accelerators Recalled for Defective Overhead Suspension Welds
Siemens is recalling 35 linear accelerator systems due to defective weld seams that could cause overhead suspensions to fall, posing a risk of severe injury.
Product
MEVATRON MD-2, MEVATRON MDX-2 and MEVATRON ME, accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1409-2017·2017-03-15
FDA Recalls Premier Guard Drape Due to Sterility Compromise
The FDA is recalling Premier Guard Drape, Sterile, because the sterile barrier was breached, compromising sterility. The product is used with RF Surgical Gauze detection systems.
Product
Premier Guard Drape, Sterile. For Use with Verisphere (01-0035) and ArQ.Sphere (01-0044) Item Number: 01-0037 Used in conjunction RF Surgical Gauze detection systems to protect scanning device from contamination during various surgical procedures
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1435-2017·2017-03-15
Siemens MEVATRON M 7400/7440 Linear Accelerators Recalled for Defective Welds
Siemens is recalling 35 MEVATRON M 7400/7440 linear accelerators because a defective weld seam could break, causing the overhead suspension to fall and potentially injure patients or others.
Product
MEVATRON M 7400/7440(MEX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1430-2017·2017-03-15
Villa Sistemi Medicali Recalls Apollo EZ X-Ray Systems Due to Footrest Detachment
Villa Sistemi Medicali is recalling 65 Apollo EZ x-ray systems because the footrest detached from the table, causing a patient to fall.
Product
Apollo EZ; Model: 9784152036 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1434-2017·2017-03-15
Siemens Medical Linear Accelerators Recalled for Defective Weld Seams
Siemens is recalling 35 MEVATRON M 6730/6740 linear accelerators because defective weld seams on overhead suspensions could break and fall, posing a risk of severe injury.
Product
MEVATRON M 6730/6740 (MEX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1280-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in AMS kits are recalled because splits or holes may compromise sterility.
Product
Catheter Pack, part number AMS4399(A
Category
Medical Device
Distribution
26 states
SevereFDA (Devices)·Z-1252-2017·2017-03-08
Olympus Uretero-reno Videoscope Recall Due to Insertion Tube Breakage
Olympus is recalling URF-V2 and URF-V2R endoscopes because the insertion tube bending section may break during surgery, causing tissue trauma.
Product
Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The URF-V2/V2R endoscopes are intended for use in endoscopic diagnosis and treatment within the ureter and kidney.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1379-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.
Product
Upper Torso Tray, part number PSS1554(B
Category
Medical Device
Distribution
26 states
SevereFDA (Devices)·Z-1329-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Product
Lap/Pelviscopy Pack, part number PSS3256(B
Category
Medical Device
Distribution
26 states
SevereFDA (Devices)·Z-1251-2017·2017-03-08
Olympus Recalls URF-P6 Uretero-reno Fiberscopes Due to Tissue Trauma Risk
Olympus is recalling URF-P6 and URF-P6R uretero-reno fiberscopes due to adverse events involving tissue trauma and stuck insertion tubes reported in similar devices.
Product
URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope
Category
Medical Device
Distribution
Distributed nationwide

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3701–3725 of 5038